NDC 70518-4500
Venlafaxine 150 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-728.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alkem Laboratories Limited | Baddi Solan, India | Makes it | Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA214127
- On the market since
- Oct 12, 2025
- Package NDCs
70518-4500-0- Official label
- DailyMed (National Library of Medicine), updated Sep 14, 2026
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